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双侧胸大肌缺损及肌肉异常一例罕见病例。

A Rare Case of Bilateral Pectoralis Major Muscle Defect and Abnormal Muscle.

作者信息

Yamamoto Mayuko, Kunihisa Tomonari, Baba Motoi, Mizumoto Sachiko, Yamashita Yuji, Miki Mayuko, Inubushi Sachiko, Okamoto Aoi, Fujimoto Ryuhei, Tanino Hirokazu

机构信息

Department of Breast Surgery, Kobe University Hospital, Kobe, Japan.

Department of Breast Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.

出版信息

Case Rep Oncol. 2022 Mar 30;15(1):351-355. doi: 10.1159/000523936. eCollection 2022 Jan-Apr.

Abstract

A 56-year-old female patient with left breast cancer presented at our hospital. Preoperative CT scan showed an isolated bilateral pectoralis major muscle defect and abnormal muscle originating from the entire sternum and inserting in the lower ribs and rectus sheath. Total mastectomy and axillary lymph node dissection were performed. We believe that this case is unique and that others like it have never been reported. If there is a defect in the pectoralis major muscle, reconstructive surgery with a tissue expander is contraindicated. Therefore, preoperative evaluation of the chest wall musculature on imaging is recommended.

摘要

一名56岁的左乳腺癌女性患者到我院就诊。术前CT扫描显示双侧胸大肌孤立性缺损,以及一块起源于整个胸骨、止于下肋和腹直肌鞘的异常肌肉。行全乳切除术和腋窝淋巴结清扫术。我们认为该病例独特,此前未见类似病例报道。如果胸大肌存在缺损,禁忌使用组织扩张器进行重建手术。因此,建议术前通过影像学对胸壁肌肉组织进行评估。

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A Rare Case of Bilateral Pectoralis Major Muscle Defect and Abnormal Muscle.双侧胸大肌缺损及肌肉异常一例罕见病例。
Case Rep Oncol. 2022 Mar 30;15(1):351-355. doi: 10.1159/000523936. eCollection 2022 Jan-Apr.
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